RGD:405237657 Rat Genome Database

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Variant: RGD:405237657 -  Homo sapiens

RGD ID: 405237657
ClinVar ID: CV2881233
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DEAF1  LOC127820019  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 686,909
GRCh38 11 686,909
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367390.1:c.27C>T
NM_001293634.1:c.664+1002C>T
NM_021008.4:c.753C>T
NG_034156.2:g.25175C>T
More... 		10/18/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003556719 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DEAF1 CLINVAR
OMIM 602635 CLINVAR